Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

Antiarrhythmic Drugs: Class III Agents as Potassium Channel Blockers01:12

Antiarrhythmic Drugs: Class III Agents as Potassium Channel Blockers

1.1K
Class III antiarrhythmic drugs are a group of medications that can prolong action potentials in the heart. They achieve this by blocking potassium channels or enhancing inward currents from sodium channels. However, these drugs have a unique property of "reverse use-dependence," which is most pronounced at slower heart rates and can lead to torsades de pointes—a specific type of arrhythmia. However, it is essential to note that excessive QT interval prolongation—a measure of...
1.1K
Dysrhythmias VI: Management of Dysrhythmias01:25

Dysrhythmias VI: Management of Dysrhythmias

25
Dysrhythmia management involves a multifaceted approach, incorporating pharmacological treatments, medical procedures, surgical interventions, lifestyle modifications, and patient education.Pharmacological ManagementAntiarrhythmic Drugs:Class I (Sodium Channel Blockers): This class includes quinidine and procainamide, which reduce the speed of impulse conduction in the heart, stabilize the cardiac membrane, and control arrhythmias. Quinidine and procainamide are Class IA agents that prolong the...
25
Antiarrhythmic Drugs: Class I Agents as Sodium Channel Blockers01:22

Antiarrhythmic Drugs: Class I Agents as Sodium Channel Blockers

1.6K
Class I antiarrhythmic drugs are used to treat various types of arrhythmias or irregular heart rhythms. These drugs block the sodium (Na+) channels in the cardiac cells, thereby affecting the movement of electrical impulses across the heart. Class I antiarrhythmic drugs are divided into three subgroups: Class IA, Class IB, and Class IC, each with distinct mechanisms of action and effects on the heart.
Class 1A Antiarrhythmic Drugs: These drugs work by moderately blocking sodium channels,...
1.6K
Disturbances in Heart Rhythm01:29

Disturbances in Heart Rhythm

1.1K
Arrhythmia or dysrhythmia refers to an abnormal heart rhythm caused by a defect in the heart's conduction system. It can cause the heart to beat irregularly, too quickly, or too slowly, leading to symptoms like chest pain, shortness of breath, and fainting. Factors such as stress, caffeine, alcohol, nicotine, cocaine, certain drugs, congenital defects, diseases, and electrolyte abnormalities can trigger arrhythmias.
Arrhythmias are categorized by their speed, rhythm, and origin. A slow heart...
1.1K
Antiarrhythmic Drugs: Class II Agents as β-Adrenergic Blockers01:24

Antiarrhythmic Drugs: Class II Agents as β-Adrenergic Blockers

805
Adrenergic stimulation generally impacts cardiac rate and rhythm. Specifically, stimulation of the β-adrenoceptors triggers an increase in intracellular calcium ion influx and pacemaker currents, which may cause arrhythmias. Catecholamines like adrenaline also demonstrate β2-adrenoceptor-mediated hypokalemia, impacting cardiac action potential and disrupting the normal cardiac rhythm. Class II antiarrhythmic drugs are β-adrenoceptor antagonists or β-blockers, which...
805
ECG Interpretation of Arrhythmias II: Atrial, Junctional and Ventricular Arrhythmias01:25

ECG Interpretation of Arrhythmias II: Atrial, Junctional and Ventricular Arrhythmias

64
Arrhythmia is a condition characterized by an irregular heart rhythm, with ECG changes that differ based on its origin and nature. The types of arrhythmias discussed below include atrial, junctional, and ventricular arrhythmias.Atrial ArrhythmiasPremature Atrial Complexes (PACs): PACs are early atrial beats caused by stress, caffeine, alcohol, electrolyte imbalances, hypoxia, hyperthyroidism, or certain medications (e.g., bronchodilators and decongestants). The ECG shows early P waves with an...
64

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Clinical Patterns and Appropriateness of Apixaban Dosing in Patients With Atrial Fibrillation.

JACC. Advances·2026
Same author

Predictors of ischemic stroke and major bleeding among patients with atrial fibrillation in clinical practice.

American heart journal·2026
Same author

Self-supervised contrastive learning enables robust electrocardiogram-based cardiac classification.

Heart rhythm O2·2026
Same author

Characteristics of a <i>Dinophysis</i> cf <i>acuminata</i> Population from a Tidewater Glacier Lagoon in a Temperate Latitude: Applications to <i>Dinophysis</i> Studies.

Marine drugs·2026
Same author

Ketamine-induced torsades de pointes: Coincidence or causality?

HeartRhythm case reports·2026
Same author

Hemodynamic Consequences and Clinical Outcomes With Intravenous Lidocaine Infusion in Patients With Atrial Fibrillation.

Journal of cardiovascular electrophysiology·2026

Related Experiment Video

Updated: Aug 9, 2025

Testing the Efficacy of Pharmacological Agents in a Pericardial Target Delivery Model in the Swine
10:05

Testing the Efficacy of Pharmacological Agents in a Pericardial Target Delivery Model in the Swine

Published on: July 7, 2016

8.4K

Protocol Development and Initial Experience With Intravenous Sotalol Loading for Atrial Arrhythmias.

Melissa L Feuerborn1, John Dechand2, Rohith S Vadlamudi1

  • 1From the Department of Medicine, University of Utah School of Medicine, Salt Lake City, UT.

Critical Pathways in Cardiology
|February 22, 2023
PubMed
Summary
This summary is machine-generated.

Intravenous (IV) sotalol loading offers a safe and effective method for treating atrial fibrillation (AF) and atrial flutter (AFL), potentially reducing hospital stays. This approach demonstrated feasibility and good tolerability in initial patient experiences.

More Related Videos

Programmed Electrical Stimulation in Mice
07:29

Programmed Electrical Stimulation in Mice

Published on: May 26, 2010

20.6K
Viral Transgene Expression in Rodent Hearts and the Assessment of Cardiac Arrhythmia Risk
05:15

Viral Transgene Expression in Rodent Hearts and the Assessment of Cardiac Arrhythmia Risk

Published on: July 27, 2022

1.7K

Related Experiment Videos

Last Updated: Aug 9, 2025

Testing the Efficacy of Pharmacological Agents in a Pericardial Target Delivery Model in the Swine
10:05

Testing the Efficacy of Pharmacological Agents in a Pericardial Target Delivery Model in the Swine

Published on: July 7, 2016

8.4K
Programmed Electrical Stimulation in Mice
07:29

Programmed Electrical Stimulation in Mice

Published on: May 26, 2010

20.6K
Viral Transgene Expression in Rodent Hearts and the Assessment of Cardiac Arrhythmia Risk
05:15

Viral Transgene Expression in Rodent Hearts and the Assessment of Cardiac Arrhythmia Risk

Published on: July 27, 2022

1.7K

Area of Science:

  • Cardiology
  • Electrophysiology
  • Pharmacology

Background:

  • Oral sotalol is a standard class III antiarrhythmic for maintaining sinus rhythm in atrial fibrillation (AF).
  • The FDA recently approved intravenous (IV) sotalol loading, primarily based on modeling data.
  • There is a need to describe protocols and clinical experience with IV sotalol loading for AF and atrial flutter (AFL).

Purpose of the Study:

  • To describe an institutional protocol for IV sotalol loading in adult patients with AF and AFL.
  • To report the initial clinical experience and outcomes of patients treated with IV sotalol loading.
  • To assess the feasibility, safety, and tolerability of IV sotalol loading for atrial arrhythmias.

Main Methods:

  • Retrospective review of patients treated with IV sotalol for AF/AFL at the University of Utah Hospital (September 2020 - April 2021).
  • Eleven patients received IV sotalol for initial loading or dose escalation.
  • Data collected included QTc intervals, hospitalization duration, cardioversion success, adverse events, and long-term therapy persistence.

Main Results:

  • Mean QTc interval increased post-infusion (mean change 42ms) but no patient discontinued medication.
  • Hospitalization duration was short (1-4 nights), with 9/11 patients undergoing electrical cardioversion.
  • No adverse events occurred during infusion or within 6 months post-discharge; 73% maintained therapy.

Conclusions:

  • A streamlined protocol for IV sotalol loading was successfully implemented for atrial arrhythmias.
  • Initial experience suggests IV sotalol loading is feasible, safe, and well-tolerated, potentially reducing hospitalization.
  • Further data are needed to support broader use of IV sotalol across diverse patient populations.